Variant #0000544488 (NC_000011.9:g.47372961dup, NM_000256.3:c.121dup (MYBPC3))

Chromosome 11
Allele Unknown
Affects function (as reported) Affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.47372961dup
DNA change (hg38) g.47351410dup
Published as MYBPC3(NM_000256.3):c.121dupC (p.R41Pfs*8)
ISCN -
DB-ID MYBPC3_000951 See all 2 reported entries
Variant remarks VKGL data sharing initiative Nederland
Reference -
ClinVar ID -
dbSNP ID -
Origin CLASSIFICATION record
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) Retrieve
Owner VKGL-NL_AMC
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_AMC
Date created 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2020-06-30 15:15:15 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
MYBPC3 NM_000256.3 +/. - c.121dup r.(?) p.(Arg41ProfsTer8)
SPI1 NM_003120.2 +/. - c.*3817dup r.(?) p.(=)


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